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Original Research

Frontiers in Environmental Science ·

Volume 14 - 2026 | https://doi.org/10.3389/fenvs.2026.1831183

Modulation of quasi-biennial oscillation by volcanic sulfate aerosols

  • Prashant Chavan1,2*corresponding author
  • Suvarna Fadnavis1
  • Anton Laakso3
  • Jean-Paul Vernier4,5,6
  • Simone Tilmes7
  • Chandran P. R. Satheesh1
  • Vijay Sagar1
  • Rolf Müller8
  1. 1Centre for Climate Change, MoES, Indian Institute of Tropical Meteorology, Pune, India
  2. 2Department of Atmospheric and Space Sciences, Savitribai Phule Pune University, Pune, India
  3. 3Finnish Meteorological Institute, Kuopio, Finland
  4. 4National Institute of Aerospace, Hampton, VA, United States
  5. 5NASA Langley Research Centre, Hampton, VA, United States
  6. 6GSMA, UMR CNRS 7331, Université de Reims Champagne-Ardenne, Reims, France
  7. 7National Center for Atmospheric Research, Boulder, CO, United States
  8. 8Forschungszentrum Jülich GmbH, ICE-4, Jülich, Germany
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Abstract

Large and moderate volcanic eruptions significantly impact the stratosphere by releasing sulfur dioxide, thereby affecting atmospheric dynamics. Mt. Pinatubo erupted in 1991 and induced a warming of 3 K in the stratosphere that led to prolonged easterly wind regimes of the Quasi-biennial oscillation (QBO). Using a three-member ensemble mean obtained from the ECHAM6-HAMMOZ model, we show the impact of eruptive volcanoes on the tropical stratosphere and the QBO from 2003 to 2013. Our simulations with volcanoes, when compared to simulations without volcanoes, show that volcanic sulfate aerosols enhanced the stratospheric aerosol optical depth (SAOD) 2 months after the eruptions of Rabaul (0.0024 ± 0.0018), Sarychev (0.0058 ± 0.0031), and Nabro (0.0075 ± 0.0053). The increase in mean tropical SAOD over the study period 2003–2013, driven by several volcanic eruptions, produced an average radiative forcing of −0.45 ± 0.21 W m -2 at the top of the atmosphere (TOA) and −0.47 ± 0.26 W m -2 at the surface in the tropical region. Volcanic aerosol precursors are injected into the tropical stratosphere through volcanic plumes, leading to an increase in sulfate aerosol concentrations of 59.6 ± 11.1 ng m -3 and heating rates of 0.05 ± 0.02 × 10 −2 K d -1 in the tropical lower stratosphere. The model simulations show that stratospheric heating caused by the volcanoes disrupts the QBO phases, resulting in the reversal of the easterly to westerly phase and vice versa. Our study shows that moderate and large volcanoes modulate the QBO.

Keywords

1 Introduction

Strong and moderate volcanic eruptions inject sulfur dioxide (SO2) gas into the stratosphere, where it forms sulfate aerosol particles (e.g., Hegerl et al., 2003). Sulfate aerosols contribute to stratospheric heating by absorbing infrared radiation, thus influencing stratospheric dynamics (Hegerl et al., 2003; Sigl et al., 2015; Santer et al., 2015). Sulfate aerosols formed from volcanic SO2 injected into the stratosphere can remain there for about 1–5 years (Carn et al., 2016). Sulfate aerosols scatter shortwave radiation, resulting in a net negative radiative forcing at the top of the atmosphere (TOA) and surface cooling (Vernier et al., 2011).

Over the past decades, multiple moderate volcanic eruptions (Volcanic Explosivity Index; VEI ≥ 3) have augmented the stratospheric aerosol load, resulting in the enhancement of SAOD and cooling of the surface (Vernier et al., 2011). Several satellite observations show an enhancement in SAOD following volcanic eruption; for example, Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) satellite data showed an increase in SAOD (0.006–0.012) following multiple volcanic eruptions during 2008–2013 (Andersson et al., 2015; Friberg et al., 2018). Similarly, combined satellite data from the Stratospheric Aerosol and Gas Experiment (SAGE–II), Global Ozone Monitoring by Occultation of Stars (GOMOS), and CALIPSO showed an increase in SAOD of 20.4 × 10−5 yr-1 from 2000–2009, primarily driven by a sequence of medium-size volcanic eruptions (Vernier et al., 2011). Several model simulation studies also reported a similar increase in SAOD by volcanic eruptions, for example, an enhancement in globally mean SAOD ∼0.007 due to volcanoes occurring globally during 2005–2014 (Schmidt et al., 2018).

The increase in SAOD following volcanic eruptions leads to a reduction in radiative forcing. For example, Schmidt et al. (2018) estimated a global mean RF of −0.08 W m-2 for 2005–2015 using CESM1-WACCM simulations performed with and without volcanic SO2 emissions. Similarly, Ge et al. (2016) reported a global mean RF of −0.10 W m-2 for 2005–2011 using GEOS-Chem simulations. Consistent with these model estimates, satellite-based observational studies also indicate reductions in global mean radiative forcing following volcanic eruptions (Andersson et al., 2015; Friberg et al., 2018).

Sulfate aerosols absorb near-infrared solar radiation and thus heat the layers in which they reside (Kremser et al., 2016; Fadnavis et al., 2021a). Model studies have reported an increase in tropical lower-stratospheric (17–35 km) heating rate following the Nabro (0.003 K d-1) and El Chichón (0.0045 K d-1) eruptions (Pitari et al., 2016; Fadnavis et al., 2021a). In addition, volcanic aerosols transported from the extratropics into the tropics can also contribute to the tropical stratospheric heating rates (Oman et al., 2006; Brühl et al., 2015; Robock, 2000; Timmreck, 2012).

The volcanic sulfate aerosol-induced heating in the stratosphere can disrupt the thermal structure (Santer et al., 2015) and influence the QBO (Bittner et al., 2016; Brenna et al., 2019; Toohey et al., 2014; Diallo et al., 2018). The impact of large volcanoes on the QBO has been reported in a few studies; e.g., Labitzke (1994) reported that Mt. Pinatubo in 1991 induced a stratospheric warming of 3 K, leading to a prolonged easterly phase of the QBO. The ECHAM5 model simulations showed a shift in the QBO phase from easterly to westerly after the Mt. Pinatubo eruption (Thomas et al., 2009). Brenna et al. (2021) reported that the Los Chocoyos eruption (VEI = 8) (14.6°N, 91.2°W) disrupted the QBO periodicity for up to 10 years. Apart from volcanic aerosols, geoengineering studies wherein the injection of 2.5–5 Tg of SO2 into the stratosphere is considered have also shown impacts on the QBO phase induced by stratospheric heating (Aquila et al., 2014; Pitari et al., 2016). Richter et al. (2017) found that in CESM1 (WACCM) simulations with an equatorial injection of 12 Tg SO2 per year, the QBO period increased by approximately 3.5 years. Past study reported a prolonged westerly phase of the QBO (Aquila et al., 2014). In extreme cases, some studies even show a complete shutdown of the QBO. For example, simulations using the ECHAM model indicate that a large injection of 8 Tg of SO2 can cause such a shutdown, while the WACCM model shows the QBO shutting down with a smaller injection of just 2 Tg of SO2 (Niemeier and Schmidt, 2017; Niemeier et al., 2020). The shutdown of the QBO depends not only on the injection rate and the model used for the simulation, but also on the injection strategy, including factors such as injection location, altitude, and injection frequency (Franke et al., 2021; Laakso et al., 2022).

Previous studies have focused on individual large tropical volcanic eruptions; here, we aim to investigate the influence of moderate volcanoes during 2003–2013 on the QBO using the state-of-the-art ECHAM6-HAMMOZ chemistry–climate model. During this period, there were a total of 17 volcanic eruptions (VEI≥3). Among these, 8 were in the tropics (20 °S – 20 °N), 7 in the northern extra-tropics (20 °N – 90 °N), and 2 in the southern extra-tropics (20 °S – 90 °S) (see Figure 1). The paper is structured as follows: Section 2 presents the model setup and details of the simulations performed for this investigation. Section 3 presents and discusses the outcomes derived from these simulations. Finally, in Section 4, the conclusions are made.

Spatial distribution of the moderate and large (VEI ≥ 3) volcanic eruptions during 2003–2013. Red stars indicate the location of volcanoes. The blue dotted line indicates the tropical region (20°S – 20°N).
Figure 1. Spatial distribution of the moderate and large (VEI ≥ 3) volcanic eruptions during 2003–2013. Red stars indicate the location of volcanoes. The blue dotted line indicates the tropical region (20°S – 20°N).

2 Model simulations and data analysis

2.1 Model description and experimental setup

We use the state-of-the-art aerosol–chemistry-climate model ECHAM6–HAMMOZ. It comprises the general circulation module ECHAM6, coupled to the aerosol and cloud microphysics module HAM (Stier et al., 2005; Schultz et al., 2018; Tegen et al., 2019). HAM predicts the nucleation, growth, evolution, and sinks of sulfate, black carbon (BC), particulate organic matter (POM), sea salt (SS), and mineral dust (DU) aerosols. The size distribution of the aerosol population is described by seven log-normal modes with prescribed variance as in the M7 aerosol module (Stier et al., 2005; Zhang et al., 2012). Moreover, HAM explicitly simulates the impact of aerosol species on cloud droplets and ice crystal formation. Other details of the model and emissions are reported by Fadnavis et al., 2017, 2019, 2021b, 2021c. Anthropogenic aerosol emissions are from the Community Emissions Data System (CEDS) (Hoesly et al., 2019). The volcanic SO2 emissions inventory used in the model simulations is based on Carn et al. (2017). The volcanic SO2 emissions used in the model are tabulated in Table 1.

TABLE 1. Volcanic SO2 (kt) emissions reaching the stratosphere and the uppermost tropical troposphere from the volcanic sulfur emission Inventory. The total annual amount and the explosive annual amount of global volcanic SO2 emissions were calculated from satellite observations from 1979 to 2014 by Carn et al. (2016).

YearTotal (kt)Explosive (kt)
2003679679
20042,997410
20054,6342,501
20061,347661
2007712122
20082,6242,318
20091,9341,379
20101,470867
20116,0304,310
2012763563
2013185180

The model simulations are performed at T63 spectral resolution, corresponding to a horizontal resolution of 1.875 ° × 1.875°. Vertically, 95 hybrid σ–p levels are used from the surface up to 0.001 hPa (approximately 90 km). The simulations have been carried out with a time step of 20°min. Monthly varying Atmospheric Model Intercomparison Project (AMIP) sea surface temperature (SST) and sea ice cover (SIC) (Taylor et al., 2000) were used as lower boundary conditions. The dust emission parameterisation is the same across all simulations and follows Tegen et al. (2002). We performed two experiments: (1) a VAL simulation, in which all aerosols, including volcanic emissions, are considered; and (2) a VAL0 simulation, in which all volcanic aerosol emissions are switched off globally. All other emissions (anthropogenic and natural) are kept the same in both experiments. Both simulations are performed for the period 2003–2013. To reduce the influence of internal variability, an ensemble-mean approach was adopted for both experiments. Three ensemble members were simulated for the period 2003–2013 after a three-year spin-up corresponding to approximately one QBO cycle (January 2000–December 2002). The ensemble members were initialized on 1, 2, and 3 January 2000 with small perturbations applied to the initial atmospheric state, and each simulation was integrated through 31 December 2013. This approach allows the ensemble members to evolve independently. In the VAL0 simulations (three ensemble members), the volcanic aerosol emissions were switched off on 1 January 2003. The VAL and VAL0 simulations ended on 31 December 2013. Each ensemble member provides daily output for the 2003–2013 simulation period. The simulations are restricted to 1 decade since simulations for longer time periods at a daily scale, extending to 80 km, are computationally expensive. To investigate the effects of volcanic aerosol during 2003–2013, we analyse the difference between VAL and VAL0 simulations. Ensemble-mean differences between the VAL and VAL0 simulations were evaluated using a two-tailed Student’s t-test at the 95% confidence level. For each month, each experiment provides approximately 30 daily values per ensemble member, resulting in about 90 samples when the three ensemble members are combined. Thus, the use of three ensemble members increases the sample size and improves the robustness of the estimated anomalies. In volcano simulations, we assumed that all volcanoes erupted at their respective times and locations. There are 17 volcanoes globally (see Figure 1) in the study period, including large and moderate volcanoes (VEI≥3) (see Table 2). VEI is used to classify the explosive magnitude of volcanic eruptions based on erupted tephra volume and eruption plume height. It is measured on a logarithmic scale from 0 to 8 (Newhall and Self, 1982).

TABLE 2. List of volcanoes from 2003 to 2013 and their Volcanic Explosivity Index (VEI).

Sr No.VolcanoMonth yearLocationVEI
1Anatahan (An)May 200316 0N. 146 0E3
2Manam (Ma)November 20044.08 0S, 145.04 0E4
3Sierra negra (Si)Oct 20051 0S 91 0W3
4Soufrière hills (So)May 200617 0N 62 0W3
5Rabaul (Ra)October 20064.27 0S, 152.20 0E4
6Jebel at tair (Je)Sep 200716 0N 42 0E3
7Chaiten (Ch)May 200842.83 0S, 72.65 0W4
8Mt okmok (Ok)July 200853.48 0N, 168.17 0W4
9Kasatochi (Ka)August 200855.00 0N, 175.00 0W4
10Redoubt (Re)Mar 200960 0N 153 0W3
11Sarychev (Sa)June 200948.00 0N, 153.20 0E4
12Eyjafjallajokull (Ey)April 201063.63 0N, 19.60 0W4
13Merapi (Me)November 20107.54 0S, 110.44 0E4
14Grimsvotn (Gr)May 201164.42 0N, 17.33 0W4
15Nabro (Na)June 201113.37 0N, 41.70 0E4
16Puyehue-cordon caulle (Pu)June 201140.59 0S, 72.12 0W5
17Etna (Et)April 201337.89 0N, 137.48 0E3

2.2 The global space-based stratospheric aerosol climatology (GloSSAC)

We compared simulated SAOD with Global Space-based Stratospheric Aerosol Climatology (GloSSAC) SAOD. The GloSSAC provides a 43–years record of stratospheric aerosol properties, focusing on aerosol extinction coefficients at 525 nm and 1020 nm. This climatology is primarily based on data from the Stratospheric Aerosol and Gas Experiment (SAGE) instruments until mid-2005, followed by the Optical Spectrograph and InfraRed Imager System (OSIRIS) and the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) until 2017 (Kovilakam et al., 2023). After 2017, the SAGE III/ISS data are used in GloSSAC. GloSSAC also integrates data from other satellite platforms, as well as ground-based, airborne, and balloon-borne instruments, to achieve a global and temporally continuous dataset (Kovilakam et al., 2023). The dataset spans from 1979 to 2023, covering latitudes from 80°S to 80°N, with a horizontal resolution of 500–1,000 km and a vertical resolution from 100 m to less than 1 km, offering a comprehensive representation of stratospheric aerosol variability (Kovilakam et al., 2023; Thomason and Knepp, 2023; NASA/LARC/SD/ASDC, 2022). Here, we used GloSSAC Version 2.2 SAOD at 525 nm from the tropopause to 40 km for the period 2003–2013 (https://asdc.larc.nasa.gov/project/GloSSAC).

3 Results

3.1 Model evaluation

Figure 2a compares the simulated global mean SAOD at 550 nm with GloSSAC observations at 525 nm during 2003–2013. The model captures the major temporal variations in SAOD, including enhanced SAOD following the Rabaul (2006), Sarychev (2009), and Nabro (2011) eruptions and low aerosol loading during the volcanically quiescent period of 2003–2005. The agreement is particularly good for the Sarychev eruption, while the model slightly underestimates the Rabaul (by ∼0.0002) and overestimates the Nabro peak (by ∼0.0013). The model simulation shows a strong correlation with GloSSAC SAOD (r = 0.87; Figure 2b), indicating that the model reasonably captures the timing and relative variability of volcanic aerosol perturbations.

**(a)** Time series global mean Stratospheric Aerosol Optical Depth (SAOD) during 2003–2013, GloSSAC at 525 nm (blue line), ECHAM-HAMMOZ at 550 nm (red line), solid vertical lines show the month of eruption. Black lines indicate eruptions in the tropical region; green lines indicate eruptions in the extratropical region. **(b)** Correlation between monthly mean SAOD from GloSSAC at 525 nm and ECHAM-HAMMOZ at 550 nm.
Figure 2. (a) Time series global mean Stratospheric Aerosol Optical Depth (SAOD) during 2003–2013, GloSSAC at 525 nm (blue line), ECHAM-HAMMOZ at 550 nm (red line), solid vertical lines show the month of eruption. Black lines indicate eruptions in the tropical region; green lines indicate eruptions in the extratropical region. (b) Correlation between monthly mean SAOD from GloSSAC at 525 nm and ECHAM-HAMMOZ at 550 nm.

Despite this good temporal agreement, there are differences in simulated SAOD and GloSSAC during 2003–2013, particularly during the volcanically quiescent period of 2003–2005 (∼0.003) and after 2012 (∼0.0025). Part of this difference arises from uncertainties in the GloSSAC record associated with satellite merging procedures, instrument transitions, and wavelength differences between GloSSAC and the model (Kovilakam et al., 2020). Also, differences are partially due to uncertainties in the model, e.g., volcanic emission inventories, transport, and aerosol optical properties (Fadnavis et al., 2013; Tilmes et al., 2023). The underestimation of model SAOD will relatively affect the simulated radiative forcing, heating rates, and QBO.

3.2 Impact of volcanoes on the SAOD, radiative forcing, and heating rates

Figure 3 illustrates simulated anomalies of SAOD (VAL-VAL0) for (1) the global mean and (2) the zonal mean averaged over the tropical region (20° S – 20° N). During the volcanically quiescent period from 2003 to 2005, SAOD anomalies increased by 0.0006 ± 0.0004 in the tropical region and by 0.00096 ± 0.00081 globally. During 2005–2013, when a series of volcanic eruptions occurred (Table 2), SAOD averaged over this period increased to 0.0014 ± 0.0011 in the tropics and 0.0023 ± 0.0019 globally.

Time series of stratospheric aerosol optical depth (SAOD) (above tropopause to 1 hPa) during 2003–2013 using ECHAM6-HAMMOZ model simulations (VAL-VAL0), Global mean (red line) and zonal mean averaged over the tropical region (blue line) (20° S - 20° N). Solid vertical lines show the month of eruption. Black lines indicate the eruption in the tropical region, and green lines indicate the eruption in the extratropical region.
Figure 3. Time series of stratospheric aerosol optical depth (SAOD) (above tropopause to 1 hPa) during 2003–2013 using ECHAM6-HAMMOZ model simulations (VAL-VAL0), Global mean (red line) and zonal mean averaged over the tropical region (blue line) (20° S - 20° N). Solid vertical lines show the month of eruption. Black lines indicate the eruption in the tropical region, and green lines indicate the eruption in the extratropical region.

Notably, Figure 3 highlights prominent SAOD peaks in 2006 (Rabaul), 2009 (Sarychev), and 2011 (Nabro) in the tropical region (Supplementary Table S1). Andersson et al. (2015) reported that the Kasatochi eruption in 2009, the Sarychev eruption in 2010, and the Nabro eruption in 2011 collectively enhanced global SAOD by 30% between 2008 and 2012 relative to the reference period 1999–2002. Our ECHAM-HAMMOZ model simulations show an increase in SAOD by 38.2% due to Kasatochi, Sarychev, and Nabro eruptions during 2008–2012, which is in good agreement with the findings of Andersson et al. (2015), indicating the reliable performance of the model. Additionally, GOMOS satellite data in the tropical region show SAOD ranging from 0.002 to 0.0055 during 2002–2008 (Vernier et al., 2011). Our model shows SAOD values ranging from 0.001 to 0.005 during the same period, which also aligns closely with the observations, indicating good agreement.

Further, we show changes in RF and heating rates caused by volcanic eruptions. Figures 4a,b show a decrease in the global mean RF at the TOA by 0.34 ± 0.17 W m-2 and by 0.45 ± 0.21 W m-2 over the tropics, averaged over the years 2003–2013. There is a reduction in global mean surface radiative forcing by 0.37 ± 0.23 W m-2 and within the tropics by 0.47 ± 0.26 W m-2 (Supplementary Figure S1). The impacts are clearly visible in the tropical mean (Figure 4b) while it is subdued in the global mean (Figure 4a). The radiative forcing within the tropical region is more negative (−0.43 ± 0.20 W m-2) than the global mean (−0.32 ± 0.16 W m-2) since the majority of volcanoes are tropical (Table 2) and solar intensity is greater in the tropics. Individual eruption contributions including Rabaul (2006), Sarychev (2009), and Nabro (2011) are summarised in Supplementary Table S1. Past studies also illustrated a similar impact of volcanic eruptions on radiative forcing. For example, the El Chichón eruption in April 1982 caused a reduction in radiative forcing by 2–4 W m−2 over a year within the region 30° S – 30° N (Robock and Mao, 1995), while the Pinatubo eruption in June 1991 reduced a TOA radiative forcing by 4.5 W m−2 within the region 40° S – 40° N (Minnis et al., 1993; Yang et al., 2019).

**(a)** Global mean radiative forcing at TOA (W m<sup>-2</sup>) (blue line), stratospheric heating rates (K d<sup>-1</sup>) × 10<sup>−2</sup> (red line) (above tropopause to 1 hPa) from VAL-VAL0 during 2003–2013, **(b)** same as **(a)** but zonally averaged over the tropical region (20° S – 20° N).
Figure 4. (a) Global mean radiative forcing at TOA (W m-2) (blue line), stratospheric heating rates (K d-1) × 10−2 (red line) (above tropopause to 1 hPa) from VAL-VAL0 during 2003–2013, (b) same as (a) but zonally averaged over the tropical region (20° S – 20° N).

Figures 4a,b also show significant enhancements in stratospheric heating rates (locally) due to volcanic sulfate aerosols. Figure 4a shows an increase in the global mean heating rates by 0.01 ± 0.009 × 10−2 K d-1, and within the tropics by 0.051 ± 0.04 × 10−2 K d-1. Similar to SAOD, the heating rate peaks are more prominent in the tropical region than in the global mean, with the largest contributions from Rabaul (2006), Sarychev (2009), and Nabro (2011) (Figure 4b; Supplementary Table S1). However, the heating rate decreased after 2012 due to the reduced amount of stratospheric sulfate aerosols (Figure 3b). Due to the higher numbers of tropical volcanoes and SAOD during the study period, the heating rates within the tropical region (0.051 ± 0.04 × 10−2) exceed the global average (0.01 ± 0.009 × 10−2 K d-1).

Further, we analyse the distribution of volcanic sulfate aerosols in the tropical stratosphere. Figure 5 illustrates the large enhancement of sulfate aerosols in the stratosphere following volcanic eruptions. This figure shows less enhancement in sulfate aerosols (23.32 ± 2 ng m-3) in the volcanically quiescent period from 2003–2004 in the VAL-VAL0 simulation. However, there is a significant enhancement by 59.60 ± 11 ng m-3 seen during 2005–2013 due to a series of moderate and large volcanoes. This figure suggests that volcanic sulfate aerosols persist for 2–3 years in the stratosphere (100–five hPa) after the eruption. The increase in stratospheric sulfate aerosol concentrations during the initial 2 months following the eruption in the tropics is presented in Supplementary Table S1. There is an enhancement in stratospheric sulfate aerosols in the tropics due to extratropical volcanoes. This may be due to transport from the extra-tropics to the tropics. It should be noted that aerosols are transported from the extratropics to the tropics and vice versa (Günther et al., 2018; Timmreck, 2012; Haywood et al., 2010; Robock, 2000). However, such analysis is out of the scope of the manuscript.

Time series of volcanic sulfate aerosol (ng m<sup>-3</sup>). The black dots indicate significance at a 95% confidence level, obtained using a Student’s t-test for the mean difference. Dotted vertical lines show the month of eruption. A thick black line in the figure indicates the tropopause.
Figure 5. Time series of volcanic sulfate aerosol (ng m-3). The black dots indicate significance at a 95% confidence level, obtained using a Student’s t-test for the mean difference. Dotted vertical lines show the month of eruption. A thick black line in the figure indicates the tropopause.

3.3 Impact of volcanic sulfate aerosol on the QBO

In this section, we show the impact of volcanic sulfate aerosol on the QBO. Figure 6a shows the altitude variation of the QBO in zonal mean zonal winds for the 5 °S – 5 °N from the VAL0 simulation. It shows that the downward propagation of the easterly is faster than (∼22–26 months cycle) the westerly (∼24–36 months cycle). Volcanoes cause a reversal of the easterly phase to the westerly phase and vice versa, as seen from the anomalies (VAL-VAL0) plotted in Figures 6b,c,d. show the time series of zonal mean zonal wind at 32 hPa and 10 hPa, respectively. In both pressure levels, the VAL0 simulation shows alternating easterly and westerly winds, completing one oscillation ∼24–30 months. In contrast, the anomalies (VAL−VAL0) are largely out of phase with VAL0 at both pressure levels. This suggests that the volcanic perturbation reverses the phase of the QBO at both pressure levels (see Figures 6c,d).

Time series of zonal wind (m s<sup>-1</sup>), **(a)** zonal wind form VAL0 simulation and averaged over the equatorial region (5° S – 5° N), **(b)** same as **(a)** but averaged form VAL - VAL0 simulation, in Figs. a–b, red shading indicates the westerly phase, and blue shading indicates the easterly phase **(c)** zonal wind at 32 hPa, **(d)** same as **(c)** but for 10 hPa.
Figure 6. Time series of zonal wind (m s-1), (a) zonal wind form VAL0 simulation and averaged over the equatorial region (5° S – 5° N), (b) same as (a) but averaged form VAL - VAL0 simulation, in Figs. a–b, red shading indicates the westerly phase, and blue shading indicates the easterly phase (c) zonal wind at 32 hPa, (d) same as (c) but for 10 hPa.

Previous studies have also reported that tropical volcanic eruptions can delay the progression of the QBO phases. For example, using the UM-UKCA aerosol-climate model, Brown et al. (2023) reported that tropical eruptions (e.g., Mt. Tambora in 1815 and Mt. Pinatubo in 1991) delayed the progression of the QBO phases. Our study extends this by considering both large and moderate volcanic eruptions globally, rather than being limited to the tropical region, allowing us to investigate the broader impact of volcanic forcing on the QBO.

Furthermore, we show the latitude pressure cross-section of the zonal mean zonal wind for the VAL0 simulation (Figure 7a). The zonal mean zonal wind shows a double-peak structure near the equator (10°S – 10°N), with maximum centred at 32 hPa and five hPa and minimum at 20 hPa (Figure 7a). A similar double-peak structure in the zonal wind at the equator is reported by Fadnavis and Beig (2009). It is produced by the secondary meridional circulation induced by the QBO (Plumb and Bell, 1982; Punge et al., 2009).

**(a)** Latitude pressure cross-section of the amplitude of QBO in zonal wind (m s<sup>-1</sup>) averaged for the period 2003–2013 from VAL0 simulation, **(b)** same as **(a)** but for VAL-VAL0 simulation, **(c)** same as **(b)** but for temperature (<sup>o</sup>C), **(d)** same as **(b)** but for H<sub>2</sub>SO<sub>4</sub> (ppt). The black hatches indicate significance at a 95% confidence level, obtained using a Student’s t-test for the mean difference.
Figure 7. (a) Latitude pressure cross-section of the amplitude of QBO in zonal wind (m s-1) averaged for the period 2003–2013 from VAL0 simulation, (b) same as (a) but for VAL-VAL0 simulation, (c) same as (b) but for temperature (oC), (d) same as (b) but for H2SO4 (ppt). The black hatches indicate significance at a 95% confidence level, obtained using a Student’s t-test for the mean difference.

When the volcanic forcing is turned on, it leads to a noticeable weakening of the zonal wind speed and increases temperature in the tropical stratosphere (32–10 hPa), while it increases zonal wind speed and decreases temperature in the upper stratosphere (five to one hPa) near the equator (Figures 7b,c). The mechanism for heating of the lower stratosphere by volcanic aerosol, which leads to QBO phase disruption, can be understood through changes in thermal-wind and residual circulation. Volcanic sulfate aerosols absorb near-infrared and longwave radiation, producing anomalous heating of the tropical lower stratosphere (Figure 7c; Supplementary Figure S2). This generates a meridional temperature gradient between the heated equatorial region and cooler subtropics (Figure 7c). Through thermal wind balance, this temperature gradient induces an equatorial positive wind shear, resulting in easterly winds (70–20 hPa) at the equator (Figure 7b). Past studies report that sulfate aerosols injected via geoengineering lead to strong heating anomalies at the equator thereby perturbing the QBO phase (Niemeier et al., 2020).

Interestingly, our results show that volcanoes lead to increased H2SO4 concentrations in the tropical lower stratosphere, where there is a decrease in wind speed and increase in temperature (32–10 hPa) (Figure 7d). The elevated H2SO4 supports chemical pathways that contribute to ozone loss in the tropical lower stratosphere (Hazra et al., 2019). However, detailed investigation of ozone chemistry is beyond the scope of this manuscript.

4 Conclusion

ECHAM6-HAMMOZ chemistry-climate model simulations for volcanic eruptions during the period 2003–2013 were analysed using the three-member ensemble mean and compared with control simulations to study the impact of volcanic sulfate aerosols on radiative forcing and the QBO. Our findings are:

  • Our simulations show that volcanoes during the study period elevated tropical SAOD by 0.0012 ± 0.00095, leading to a negative radiative forcing in the tropical region (20 °S – 20 °N) (TOA: −0.45 ± 0.21 W m-2; surface: −0.47 ± 0.26 W m-2). Comparison of our findings with other models shows slight differences in simulated SOAD and radiative forcing values. For example, Brühl et al. (2015) using the EMAC model reported an increase in SAOD by 0.001–0.01 in the tropics for tropical volcanic eruptions from 2002 to 2012, producing a decrease in radiative forcing by −0.1 to −0.26 W m-2. Schmidt et al. (2018) using the CESM1-WACCM model estimated an enhancement in SAOD by 0.0076 during 2005–2014 that caused a reduction in global mean radiative forcing by −0.10 W m-2. The differences between model results arise from variations in volcanic SO2 inventory, injection methodology, and the aerosol parameterization, used in the model (Mills et al., 2016).
  • The volcanic eruptions increased the sulfate aerosol amount in the tropical lower stratosphere by 56.60 ± 11 ng m-3 during 2003–2013. These aerosols enter the tropical stratosphere and elevate the lower stratospheric heating by 0.05 ± 0.02 × 10−2 K d-1. This heating contributes to the reversal of the easterly to westerly phases of the QBO and vice versa.
  • Volcanic sulfate aerosols lead to a strengthening of QBO wind speeds at ∼5 hPa and a weakening at ∼20 hPa near the equator, accompanied by increased temperatures and enhanced H2SO4 concentrations in the same region. The enhanced H2SO4 concentrations in the lower stratosphere may lead to ozone loss.

Our study points out that moderate and large volcanoes modulate the QBO. However, the results may vary from model to model. The uncertainties in a particular model arise from the use of emission inventories, transport processes, and various parametrizations (Fadnavis et al., 2013; 2017; 2019). These uncertainties can affect the simulated SAOD, radiative forcing, heating rates, and QBO response. The QBO modulates tropical convection and cyclones, causing an impact on extreme weather (Fadnavis et al., 2011; Kroll et al., 2024). Hence, representation of volcanic aerosol forcing and its interaction with the QBO may improve climate projections.

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Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fenvs.2026.1831183/full#supplementary-material

Supplementary material Supplementary material at the source

Footnotes

Edited by: Baijun Tian, NASA Jet Propulsion Laboratory (JPL), United States

Reviewed by: Ioannis Konstantinos Christodoulakis, American College of Greece, Greece

Frank Arthur, University of Leeds, United Kingdom

Statements

Conflict of interest

Author RM was employed by Forschungszentrum Jülich GmbH.

The remaining author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The author SF declared that they were an editorial board member of Frontiers at the time of submission. This had no impact on the peer review process and the final decision.

Funding

The author(s) declared that financial support was not received for this work and/or its publication.

Data availability

The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.

Author contributions

PC: Validation, Writing – original draft, Formal Analysis, Conceptualization, Writing – review and editing, Methodology, Data curation, Software, Investigation, Visualization. SF: Methodology, Supervision, Conceptualization, Investigation, Writing – review and editing. AL: Writing – review and editing, Methodology, Supervision. J-PV: Supervision, Writing – review and editing, Methodology. ST: Writing – review and editing, Supervision, Methodology. CS: Writing – review and editing, Visualization, Methodology, Software. VS: Data curation, Validation, Visualization, Writing – review and editing. RM: Methodology, Writing – review and editing, Supervision.

Acknowledgements

The authors thank the staff of the High-Power Computing Centre (HPC) in IITM, Pune, India, for providing computer resources.

References

  1. Andersson S. M., Martinsson B. G., Vernier J. P., Friberg J., Brenninkmeijer C. A. M., Hermann M. (2015). Significant radiative impact of volcanic aerosol in the lowermost stratosphere. Nat. Commun. 6, 1 – 8. doi:10.1038/ncomms8692
  2. Aquila V., Garfinkel C. I., Newman P. A., Oman L. D., Waugh D. W. (2014). Modifications of the quasi-biennial oscillation by a geoengineering perturbation of the stratospheric aerosol layer. Geophys. Res. Lett. 41, 1738 – 1744. doi:10.1002/2013GL058818
  3. Bittner M., Schmidt H., Timmreck C., Sienz F. (2016). Using a large ensemble of simulations to assess the Northern Hemisphere stratospheric dynamical response to tropical volcanic eruptions and its uncertainty. Geophys. Res. Lett. 43, 9324 – 9332. doi:10.1002/2016GL070587
  4. Brenna H., Kutterolf S., Krüger K. (2019). Global ozone depletion and increase of UV radiation caused by pre-industrial tropical volcanic eruptions. Sci. Rep. 9, 1 – 14. doi:10.1038/s41598-019-45630-0
  5. Brenna H., Kutterolf S., Mills M. J., Niemeier U., Timmreck C., Krüger K. (2021). Decadal disruption of the QBO by tropical volcanic supereruptions. Geophys. Res. Lett. 48 (5), e2020GL089687. doi:10.1029/2020GL089687
  6. Brown F., Marshall L., Haynes P. H., Garcia R. R., Birner T., Schmidt A. (2023). On the magnitude and sensitivity of the quasi-biennial oscillation response to a tropical volcanic eruption. Atmos. Chem. Phys. 23, 5335 – 5353. doi:10.5194/acp-23-5335-2023
  7. Brühl C., Lelieveld J., Tost H., Höpfner M., Glatthor N. (2015). Stratospheric sulfur and its implications for radiative forcing simulated by the chemistry climate model EMAC. J. Geophys. Res. 120, 2103 – 2118. doi:10.1002/2014JD022430
  8. Carn S. A., Clarisse L., Prata A. J. (2016). Multi-decadal satellite measurements of global volcanic degassing. J. Volcanol. Geotherm. Res. 311, 99 – 134. doi:10.1016/j.jvolgeores.2016.01.002
  9. Carn S. A., Fioletov V. E., Mclinden C. A., Li C., Krotkov N. A. (2017). A decade of global volcanic SO 2 emissions measured from space. Sci. Rep. 7, 1 – 12. doi:10.1038/srep44095
  10. Diallo M., Riese M., Birner T., Konopka P., Müller R., Hegglin M. I. (2018). Response of stratospheric water vapor and ozone to the unusual timing of El Niño and the QBO disruption in 2015-2016. Atmos. Chem. Phys. 18, 13055 – 13073. doi:10.5194/acp-18-13055-2018
  11. Fadnavis S., Beig G. (2009). Quasi-biennial oscillation in ozone and temperature over tropics. J. Atmos. Solar-Terrestrial Phys. 71, 257 – 263. doi:10.1016/j.jastp.2008.11.012
  12. Fadnavis S., Chakraborty T., Ghude S. D., Beig G., Ernest Raj P. (2011). Modulation of cyclone tracks in the Bay of Bengal by QBO. J. Atmos. Solar-Terrestrial Phys. 73, 1868 – 1875. doi:10.1016/j.jastp.2011.04.014
  13. Fadnavis S., Semeniuk K., Pozzoli L., Schultz M. G., Ghude S. D., Das S. (2013). Transport of aerosols into the UTLS and their impact on the Asian monsoon region as seen in a global model simulation. Atmos. Chem. Phys. 13, 8771 – 8786. doi:10.5194/acp-13-8771-2013
  14. Fadnavis S., Roy C., Sabin T. P., Ayantika D. C., Ashok K. (2017). Potential modulations of pre-monsoon aerosols during El Niño: impact on Indian summer monsoon. Clim. Dyn. 49, 2279 – 2290. doi:10.1007/s00382-016-3451-6
  15. Fadnavis S., Sabin T. P., Roy C., Rowlinson M., Rap A., Vernier J. P. (2019). Elevated aerosol layer over South Asia worsens the Indian droughts. Sci. Rep. 9, 1 – 11. doi:10.1038/s41598-019-46704-9
  16. Fadnavis S., Müller R., Chakraborty T., Sabin T. P., Laakso A., Rap A. (2021a). The role of tropical volcanic eruptions in exacerbating Indian droughts. Sci. Rep. 11, 1 – 13. doi:10.1038/s41598-021-81566-0
  17. Fadnavis S., Sioris C. E., Wagh N., Chattopadhyay R., Tao M., Chavan P. (2021b). A rising trend of double tropopauses over South Asia in a warming environment: implications for moistening of the lower stratosphere. Int. J. Climatol. 41, E200 – E215. doi:10.1002/joc.6677
  18. Fadnavis S., Sabin T. P., Rap A., Müller R., Kubin A., Heinold B. (2021c). The impact of COVID-19 lockdown measures on the Indian summer monsoon. Environ. Res. Lett. 16, 074054. doi:10.1088/1748-9326/ac109c
  19. Franke H., Niemeier U., Visioni D. (2021). Differences in the quasi-biennial oscillation response to stratospheric aerosol modification depending on injection strategy and species. Atmos. Chem. Phys. 21, 8615 – 8635. doi:10.5194/acp-21-8615-2021
  20. Friberg J., Martinsson B. G., Andersson S. M., Sandvik O. S. (2018). Volcanic impact on the climate - the stratospheric aerosol load in the period 2006-2015. Atmos. Chem. Phys. 18, 11149 – 11169. doi:10.5194/acp-18-11149-2018
  21. Ge C., Wang J., Carn S., Yang K., Ginoux P., Krotkov N. (2016). Satellite-based global volcanic SO2 emissions and sulfate direct radiative forcing during 2005–2012. J. Geophys. Res. 121, 3446 – 3464. doi:10.1002/2015JD023134
  22. Günther A., Höpfner M., Sinnhuber B. M., Griessbach S., Deshler T., Von Clarmann T. (2018). MIPAS observations of volcanic sulfate aerosol and sulfur dioxide in the stratosphere. Atmos. Chem. Phys. 18, 1217 – 1239. doi:10.5194/acp-18-1217-2018
  23. Haywood J. M., Jones A., Clarisse L., Bourassa A., Barnes J., Telford P. (2010). Observations of the eruption of the sarychev volcano and simulations using the HadGEM2 climate model. J. Geophys. Res. 115, 1 – 18. doi:10.1029/2010JD014447
  24. Hazra M. K., Ghoshal S., Mahata P. (2019). Sulfuric acid decomposition chemistry above junge layer in earth's atmosphere concerning ozone depletion and healing. Commun. Chem. 2, 75. doi:10.1038/s42004-019-0178-4
  25. Hegerl G. C., Crowley T. J., Baum S. K., Kim K. Y., Hyde W. T. (2003). Detection of volcanic, solar and greenhouse gas signals in paleo-reconstructions of Northern Hemispheric temperature. Geophys. Res. Lett. 30, 94 – 97. doi:10.1029/2002gl016635
  26. Hoesly R., O'Rourke P., Braun C., Feng L., Smith S. J., Pitkanen T. (2019). CEDS: Community Emissions Data System. Geneva, Switzerland: Zenodo. doi:10.5281/zenodo.3592073
  27. Kovilakam M., Thomason L. W., Ernest N., Rieger L., Bourassa A., Millán L. (2020). The Global Space-based stratospheric aerosol climatology (version 2.0): 1979–2018. Earth Syst. Sci. Data 12, 2607 – 2634. doi:10.5194/essd-12-2607-2020
  28. Kovilakam M., Thomason L., Knepp T. (2023). SAGE III/ISS aerosol/cloud categorization and its impact on GloSSAC. Atmos. Meas. Tech. 16, 2709 – 2731. doi:10.5194/amt-16-2709-2023
  29. Kremser S., Thomason L. W., von Hobe M., Hermann M., Deshler T., Timmreck C. (2016). Stratospheric aerosol—Observations, processes, and impact on climate. Rev. Geophys. 54, 278 – 335. doi:10.1002/2015RG000511
  30. Kroll C. A., Fueglistaler S., Schmidt H., Dauhut T., Timmreck C. (2024). The impact of stratospheric aerosol heating on the frozen hydrometeor transport pathways in the tropical tropopause layer. Environ. Res. Lett. 19, 044008. doi:10.1088/1748-9326/ad33d0
  31. Laakso A., Niemeier U., Visioni D., Tilmes S., Kokkola H. (2022). Dependency of the impacts of geoengineering on the stratospheric sulfur injection strategy-part 1: intercomparison of modal and sectional aerosol modules. Atmos. Chem. Phys. 22, 93 – 118. doi:10.5194/acp-22-93-2022
  32. Labitzke K. (1994). Stratospheric temperature changes after the pinatubo eruption. J. Atmos. Solar-Terrestrial Phys. 56, 1027 – 1034. doi:10.1016/0021-9169(94)90039-6
  33. Mills M. J., Schmidt A., Easter R., Solomon S., Kinnison D. E., Ghan S. J. (2016). Global volcanic aerosol properties derived from emissions, 1990–2014, using CESM1(WACCM). J. Geophys. Res. 121, 2332 – 2348. doi:10.1002/2015JD024290
  34. Minnis P., Harrison E. F., Stowe L. L., Gibson G. G., Denn F. M., Doelling D. R. (1993). Radiative climate forcing by the Mount Pinatubo eruption. Science 259, 1411 – 1415. doi:10.1126/science.259.5100.1411
  35. NASA/LARC/SD/ASDC (2022). Global space-based stratospheric aerosol climatology version 2.2. doi:10.5067/GLOSSAC-L3-V2.2
  36. Newhall C. G., Self S. (1982). The volcanic explosivity index (VEI): an estimate of explosive magnitude for historical volcanism. J. Geophys. Res. Oceans 87 (C2), 1231 – 1238. doi:10.1029/JC087iC02p01231
  37. Niemeier U., Schmidt H. (2017). Changing transport processes in the stratosphere by radiative heating of sulfate aerosols. Atmos. Chem. Phys. 17, 14871 – 14886. doi:10.5194/acp-17-14871-2017
  38. Niemeier U., Richter J. H., Tilmes S. (2020). Differing responses of the quasi-biennial oscillation to artificial SO 2 injections in two global models. Atmos. Chem. Phys. 20 (14), 8975 – 8987. doi:10.5194/acp-20-8975-2020
  39. Oman L., Robock A., Stenchikov G. L., Thordarson T., Koch D., Shindell D. T. (2006). Modeling the distribution of the volcanic aerosol cloud from the 1783-1784 laki eruption. J. Geophys. Res. Atmos. 111, 1 – 15. doi:10.1029/2005JD006899
  40. Pitari G., Di Genova G., Mancini E., Visioni D., Gandolfi I., Cionni I. (2016). Stratospheric aerosols from major volcanic eruptions: a composition-climate model study of the aerosol cloud dispersal and e-folding time. Atmos. (Basel) 7 (6), 75. doi:10.3390/atmos7060075
  41. Plumb R. A., Bell R. C. (1982). A model of the quasi‐biennial oscillation on an equatorial beta‐plane. Q. J. R. Meteorological Soc. 108, 335 – 352. doi:10.1002/qj.49710845604
  42. Punge H. J., Konopka P., Giorgetta M. A., Müller R. (2009). Effects of the quasi-biennial oscillation on low-latitude transport in the stratosphere derived from trajectory calculations. J. Geophys. Res. Atmos. 114, 1 – 16. doi:10.1029/2008JD010518
  43. Richter J. H., Tilmes S., Mills M. J., Tribbia J. J., Kravitz B., MacMartin D. G. (2017). Stratospheric dynamical response and ozone feedbacks in the presence of SO 2 injections. J. Geophys. Res. Atmos. 122 (23), 12557 – 12573. doi:10.1002/2017JD026912
  44. Robock A. (2000). Volcanic eruptions and climate. Rev. Geophys. 38, 191 – 219. doi:10.1029/1998RG000054
  45. Robock A., Mao J. (1995). The volcanic signal in surface temperature observations. J. Clim. 8, 1086 – 1103. doi:10.1175/1520-0442(1995)008<1086:TVSIST>2.0.CO;2
  46. Santer B. D., Solomon S., Bonfils C., Zelinka M. D., Painter J. F., Beltran F. (2015). Observed multivariable signals of late 20th and early 21st century volcanic activity. Geophys. Res. Lett. 42, 500 – 509. doi:10.1002/2014GL062366
  47. Schmidt A., Mills M. J., Ghan S., Gregory J. M., Allan R. P., Andrews T. (2018). Volcanic radiative forcing from 1979 to 2015. J. Geophys. Res. Atmos. 123 (22), 12491 – 12508. doi:10.1029/2018JD028776
  48. Schultz M. G., Stadtler S., Schröder S., Taraborrelli D., Franco B., Krefting J. (2018). The chemistry–climate model ECHAM6.3-HAM2.3-MOZ1.0. Geosci. Model Dev. 11, 1695 – 1723. doi:10.5194/gmd-11-1695-2018
  49. Sigl M., Winstrup M., McConnell J. R., Welten K. C., Plunkett G., Ludlow F. (2015). Timing and climate forcing of volcanic eruptions for the past 2,500 years. Nature 523, 543 – 549. doi:10.1038/nature14565
  50. Stier P., Feichter J., Kinne S., Kloster S., Vignati E., Wilson J. (2005). The aerosol-climate model ECHAM5-HAM. Atmos. Chem. Phys. 5, 1125 – 1156. doi:10.5194/acp-5-1125-2005
  51. Taylor K. E., Williamson D. L., Zwiers F. W. (2000). The sea surface temperature and sea-ice concentration boundary conditions for AMIP II simulations, program for climate model diagnosis and intercomparison (PCMDI). Lawrence Livermore Natl. Lab. Livermore, Calif. Rep. 60, 1 – 28.
  52. Tegen I., Harrison S. P., Kohfeld K., Prentice I. C., Coe M., Heimann M. (2002). Impact of vegetation and preferential source areas on global dust aerosol: results from a model study. J. Geophys. Res. Atmos. 107 (D21), 4576. doi:10.1029/2001JD000963
  53. Tegen I., Neubauer D., Ferrachat S., Drian C. S., Bey I., Schutgens N. (2019). The global aerosol-climate model echam6.3-ham2.3 -Part 1: aerosol evaluation. Geosci. Model Dev. 12, 1643 – 1677. doi:10.5194/gmd-12-1643-2019
  54. Thomas M. A., Giorgetta M. A., Timmreck C., Graf H. F., Stenchikov G. (2009). Simulation of the climate impact of Mt. Pinatubo eruption using ECHAM5-Part 2: sensitivity to the phase of the QBO and ENSO. Atmos. Chem. Phys. 9, 3001 – 3009. doi:10.5194/acp-9-3001-2009
  55. Thomason L. W., Knepp T. (2023). Quantifying SAGE II (1984-2005) and SAGE III/ISS (2017-2022) observations of smoke in the stratosphere. Atmos. Chem. Phys. 23, 10361 – 10381. doi:10.5194/acp-23-10361-2023
  56. Tilmes S., Mills M. J., Zhu Y., Bardeen C. G., Vitt F., Yu P. (2023). Description and performance of a sectional aerosol microphysical model in the community earth system model (CESM2). Geosci. Model Dev. 16, 6087 – 6125. doi:10.5194/gmd-16-6087-2023
  57. Timmreck C. (2012). Modeling the climatic effects of large explosive volcanic eruptions. WIREs Clim. Change 3, 545 – 564. doi:10.1002/wcc.192
  58. Toohey M., Krüger K., Bittner M., Timmreck C., Schmidt H. (2014). The impact of volcanic aerosol on the Northern Hemisphere stratospheric polar vortex: mechanisms and sensitivity to forcing structure. Atmos. Chem. Phys. 14, 13063 – 13079. doi:10.5194/acp-14-13063-2014
  59. Vernier J. P., Thomason L. W., Pommereau J. P., Bourassa A., Pelon J., Garnier A. (2011). Major influence of tropical volcanic eruptions on the stratospheric aerosol layer during the last decade. Geophys. Res. Lett. 38, 1 – 8. doi:10.1029/2011GL047563
  60. Yang W., Vecchi G. A., Fueglistaler S., Horowitz L. W., Luet D. J., Muñoz Á. G. (2019). Climate impacts from large volcanic eruptions in a high-resolution climate model: the importance of forcing structure. Geophys. Res. Lett. 46, 7690 – 7699. doi:10.1029/2019GL082367
  61. Zhang K., O’Donnell D., Kazil J., Stier P., Kinne S., Lohmann U. (2012). The global aerosol-climate model ECHAM-HAM, version 2: sensitivity to improvements in process representations. Atmos. Chem. Phys. 12, 8911 – 8949. doi:10.5194/acp-12-8911-2012

Citation

Chavan, P., et al. (2026). Modulation of quasi-biennial oscillation by volcanic sulfate aerosols. Frontiers in Environmental Science, Volume 14. https://doi.org/
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Copyright © 2026 Chavan, Fadnavis, Laakso, Vernier, Tilmes, Satheesh, Sagar and Müller.

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*Correspondence: Prashant Chavan

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